rs104894223

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs104894223(A;G)

Make rs104894223(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

86951990

Gene	FZD4, PRSS23

is a	snp
is	mentioned by
dbSNP	rs104894223
dbSNP (classic)	rs104894223
ClinGen	rs104894223
ebi	rs104894223
HLI	rs104894223
Exac	rs104894223
Gnomad	rs104894223
Varsome	rs104894223
LitVar	rs104894223
Map	rs104894223
PheGenI	rs104894223
Biobank	rs104894223
1000 genomes	rs104894223
hgdp	rs104894223
ensembl	rs104894223
geneview	rs104894223
scholar	rs104894223
google	rs104894223
pharmgkb	rs104894223
gwascentral	rs104894223
openSNP	rs104894223
23andMe	rs104894223
SNPshot	rs104894223
SNPdbe	rs104894223
MSV3d	rs104894223
GWAS Ctlg	rs104894223

Max Magnitude

0

OMIM	604579
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894223(G;G)
Alt	rs104894223(G;G)
Reference	Rs104894223(A;A)
Significance	Pathogenic
Disease	Retinopathy of prematurity
Variation	info
Gene	PRSS23 FZD4
CLNDBN	Retinopathy of prematurity
Reversed	1
HGVS	NC_000011.9:g.86663032T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005824.2,